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Adsorption characteristics of bovine serum albumin onto alumina with a specific crystalline structure

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Abstract

Bone cement containing alumina particles with a specific crystalline structure exhibits the ability to bond with bone. These particles (AL-P) are mainly composed of delta-type alumina (δ-Al2O3). It is likely that some of the proteins present in the body environment are adsorbed onto the cement and influence the expression of its bioactivity. However, the effect that this adsorption of proteins has on the bone-bonding mechanism of bone cement has not yet been elucidated. In this study, we investigated the characteristics of the adsorption of bovine serum albumin (BSA) onto AL-P and compared them with those of its adsorption onto hydroxyapatite (HA), which also exhibits bone-bonding ability, as well as with those of adsorption onto alpha-type alumina (α-Al2O3), which does not bond with bone. The adsorption characteristics of BSA onto AL-P were very different from those onto α-Al2O3 but quite similar to those onto HA. It is speculated that BSA is adsorbed onto AL-P and HA by interionic interactions, while it is adsorbed onto α-Al2O3 by electrostatic attraction. The results suggest that the specific adsorption of albumin onto implant materials might play a role in the expression of the bone-bonding abilities of the materials.

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Acknowledgments

This work was partially supported by a research grant from the Inamori Foundation, Japan and a Grant-in-Aid for Scientific Research from The Ministry of Education, Culture, Sports, Science and Technology, Japan. The authors thank Mr. Okano and Mr. Kaji, Taihei Chemical Industrial Co. Ltd., for providing the HA powder. They also thank Prof. Ishida, Tohoku University, and Dr. Maeda, Nagoya Institute of Technology, for the use of the instrument to measure the specific surface areas.

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Correspondence to Masakazu Kawashita.

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Kawashita, M., Hayashi, J., Li, Z. et al. Adsorption characteristics of bovine serum albumin onto alumina with a specific crystalline structure. J Mater Sci: Mater Med 25, 453–459 (2014). https://doi.org/10.1007/s10856-013-5086-z

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  • DOI: https://doi.org/10.1007/s10856-013-5086-z

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